A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree. Issue 5 (20th March 2019)
- Record Type:
- Journal Article
- Title:
- A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree. Issue 5 (20th March 2019)
- Main Title:
- A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree
- Authors:
- Cheng, Jingliang
Fu, Jiewen
Zhou, Qi
Xiang, Xiaohong
Wei, Chunli
Yang, Lisha
Fu, Shangyi
Khan, Md. Asaduzzaman
Lv, Hongbin
Fu, Junjiang - Abstract:
- Is Part Of:
- Journal of cellular and molecular medicine. Volume 23:Issue 5(2019)
- Journal:
- Journal of cellular and molecular medicine
- Issue:
- Volume 23:Issue 5(2019)
- Issue Display:
- Volume 23, Issue 5 (2019)
- Year:
- 2019
- Volume:
- 23
- Issue:
- 5
- Issue Sort Value:
- 2019-0023-0005-0000
- Page Start:
- 3776
- Page End:
- 3780
- Publication Date:
- 2019-03-20
- Subjects:
- Cytology
Medicine
Molecular Biology
Cytologie -- Périodiques
Médecine -- Périodiques
Biologie moléculaire -- Périodiques
Cytology -- Periodicals
Medicine -- Periodicals
Molecular biology -- Periodicals
611.01805 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1582-4934 ↗
http://www.blackwell-synergy.com/loi/jcmm ↗
http://www.usc.edu/hsc/nml/e-resources/info/joucelmm.html ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jcmm.14278 ↗
- Languages:
- English
- ISSNs:
- 1582-1838
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.005000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 17480.xml